R-X-Fix
Country not established
- Devices
- 1
What R-X-Fix makes
R-X-Fix manufactures the R-X-FIX External Fixator, a device used for stabilizing and aligning fractured bones through external skeletal fixation, commonly applied in orthopedic trauma and reconstructive surgery.
The company’s portfolio is regulated under FDA Class II devices, with the R-X-FIX External Fixator authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
R-X-Fix External Fixator Ref K051017
510(k) 510(k)
Frequently asked questions
How many devices does R-X-Fix have in the registry?
The registry currently lists 1 device for R-X-Fix. Devices recorded under merged duplicate company entries are counted once.
Which registries list R-X-Fix's devices?
Among its 1 most recently registered device, R-X-Fix has devices listed in FDA 510(k) (1 device).
What risk classes do R-X-Fix's devices fall under?
Among its 1 most recently registered device, the classes recorded for R-X-Fix's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from R-X-Fix in the registry?
The most recently registered devices listed for R-X-Fix include R-X-FIX EXTERNAL FIXATOR.